Chloramine T trihydrate - ≥98% , CAS No.7080-50-4

CAS: 7080-50-4 Cat. No.: C1506838 Formula: C7H7CINNaO2S·3H2O Peso molecolare: 281.69 Beilstein Registry Number: 3924168 Numero EC: 615-172-8
Disponibile su ordine
GRADE & PURITY ≥98%
Synonyms
Chloraseptin | Euclorina | Euclorina | Benzenesulfonamide, N-chloro-4-methyl-, sodium salt, trihydrate | Disifin | HALAMID AQUA | p-Toluenesulfonchloramide Sodium Salt | HY-U00087 | Sodium derivative of N-chloro-p-toluenesulfonamide trihydrate | CHLORAMIN
Storage
Protected from light,Room temperature,Argon charged
Shipped In
Normal
★
Size
Germania (EU)
USA*
Price
Qty
250g
C1506838-250g
Su ordinazione · 8–12 settimane
23,34€
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Protected from light,Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Chloramine T (CAT) trihydrate is a commonly used reagent for organic synthesis especially in heterocyclic chemistry. CAT is an active chlorine compound that shows antimicrobial activity.
for the detection of halogens and bromate;Chloramine T trihydrate may be used as an oxidizing agent in the synthesis of 8-chloro-[1,2,4]triazolo[4,3-a]pyrazine derivatives and novel isoxazolines.
It may also be used in the synthesis of the following compounds:
· Nitrile imines by the oxidative dehydrogenation of N-(nitrobenzyl)-imidazole aldehyde hydrazine.
· Mono-N-tosylated-1,2-diamines.
· 3,5-Disubstituted isoxazoles.
· Fused 3,6-disubstituted triazolothiadiazoles by the oxidative cyclization of N-heteroaryl-substituted hydrazones.
Nitrene source for aziridinations and aminohydroxylations.
Chloramine T (CAT) trihydrate is a commonly used reagent for organic synthesis especially in heterocyclic chemistry. CAT is an active chlorine compound that shows antimicrobial activity.
for the detection of halogens and bromate;Chloramine T trihydrate may be used as an oxidizing agent in the synthesis of 8-chloro-[1,2,4]triazolo[4,3-a]pyrazine derivatives and novel isoxazolines.
It may also be used in the synthesis of the following compounds:
· Nitrile imines by the oxidative dehydrogenation of N-(nitrobenzyl)-imidazole aldehyde hydrazine.
· Mono-N-tosylated-1,2-diamines.
· 3,5-Disubstituted isoxazoles.
· Fused 3,6-disubstituted triazolothiadiazoles by the oxidative cyclization of N-heteroaryl-substituted hydrazones.
Nitrene source for aziridinations and aminohydroxylations.

Specifications

Sinonimi
Chloraseptin | Euclorina | Euclorina | Benzenesulfonamide, N-chloro-4-methyl-, sodium salt, trihydrate | Disifin | HALAMID AQUA | p-Toluenesulfonchloramide Sodium Salt | HY-U00087 | Sodium derivative of N-chloro-p-toluenesulfonamide trihydrate | CHLORAMIN
Specifiche e purezza
≥98%
Condizioni di conservazione di stoccaggio
Protected from light,Room temperature,Argon charged
Spedito in
Normal
Purezza
≥98%
Nomi e identificatori
Sorrisi canonici
CC1=CC=C(C=C1)S(=O)(=O)[N-]Cl.O.O.O.[Na+]
IUPAC Name
sodium;chloro-(4-methylphenyl)sulfonylazanide;trihydrate
InChIKey
NZYOAGBNMCVQIV-UHFFFAOYSA-N
INCHI
1S/C7H7ClNO2S.Na.3H2O/c1-6-2-4-7(5-3-6)12(10,11)9-8;;;;/h2-5H,1H3;;3*1H2/q-1;+1;;;
Isomeri SMILES
CC1=CC=C(C=C1)S(=O)(=O)[N-]Cl.O.O.O.[Na+]
WGK Germania
2
CAS alternativo
127-65-1
Numero UN
3263
Peso molecolare
281.69
Beilstein
3924168

Documentazione

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassBenzenesulfonamides
Intermediate Tree Nodes Not available
Direct ParentBenzenesulfonamides
Alternative Parents Tosyl compounds  Benzenesulfonyl compounds  Sulfonyls  Organosulfonic acids and derivatives  Organic metal halides  Organic sodium salts  Organic oxides  Organic nitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzenesulfonamide - Tosyl compound - Benzenesulfonyl group - Toluene - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Organic metal halide - Organic alkali metal salt - Organic sodium salt - Organic salt - Organic oxygen compound - Organosulfur compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as benzenesulfonamides. These are organic compounds containing a sulfonamide group that is S-linked to a benzene ring.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

3 results found

Lot NumberCertificate TypeDataOggetto
C2606420Certificate of AnalysisMar 16, 2026 C1506838
C2606422Certificate of AnalysisMar 16, 2026 C1506838
C2606423Certificate of AnalysisMar 16, 2026 C1506838
Proprietà chimiche e fisiche
SolubilitàSoluble in water and ethyl alcohol. Insoluble in benzene and ethers.
SensibilitàLight sensitive.Air & Moisture Sensitive
Punto di infiammabilità (°F)377.6 °F
Punto di infiammabilità (°C)192 °C
Punto di fusione (°C)167-170°C
Peso molecolare281.690 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count1
Exact Mass281.01 Da
Monoisotopic Mass281.01 Da
Topological Polar Surface Area46.500 Ų
Heavy Atom Count16
Formal Charge0
Complexity231.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count5
Domande frequenti e articoli
Citations of This Product
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

Domande frequenti

What is the purity of this product?
This product is supplied at ≥98% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store at room temperature, protected from light, under argon. It is supplied under an argon blanket; reseal under inert gas after each use.
How is this product shipped?
This product ships under standard ambient conditions. No temperature-controlled packaging is required.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 7080-50-4, the molecular formula is C7H7ClNNaO2S·3H2O, and the molecular weight is 281.69 g/mol. InChIKey NZYOAGBNMCVQIV-UHFFFAOYSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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